Interim GMP Facilities Director Consultant
About The Role
We are partnering with an established life sciences company seeking an Interim GMP Facilities Director Consultant in Minnetonka, MN. This hands-on leader will oversee daily facilities operations, maintenance, critical building systems, and ongoing projects within a GMP manufacturing environment. The consultant will guide an established team, maintain operational continuity, and partner with Manufacturing, Quality, Engineering, and EHS. The initial engagement is approximately 90 days, with an immediate start and five days onsite each week. There is potential for consideration for a permanent Director role based on mutual interest and fit.
**5 days onsite per week**
**Must have extensive pharma/biotech/medical device GMP manufacturing background**
Primary Responsibilities
-
Lead daily facilities operations, prioritize site needs, and provide clear direction to facilities staff and service providers.
-
Oversee preventive maintenance, calibration, and repair programs for building systems, utilities, and manufacturing and testing equipment.
-
Maintain accurate maintenance records and GMP documentation through the computerized maintenance management system (CMMS).
-
Keep facilities and equipment ready for inspections; support audits and manage facilities-related deviations, corrective actions, and change controls.
-
Coordinate with Manufacturing, Engineering, Validation, and Quality on equipment installation, qualification, and operational readiness.
-
Manage active construction, renovation, and equipment projects, including contractor performance, schedules, and budgets.
-
Oversee facilities spending, vendor relationships, contracted services, and building maintenance obligations.
-
Support workplace safety, site security, and business continuity for critical facilities systems.
Candidate Qualifications
-
Bachelor`s degree in Engineering, Facilities Management, or a related discipline, or equivalent professional experience.
-
At least 12 years of facilities and engineering experience within GMP-regulated pharmaceutical, biotechnology, or medical device manufacturing.
-
At least five years leading facilities teams, including experience managing managers and supporting multiple locations.
-
At least five years managing construction, expansion, or renovation projects in regulated environments.
-
Extensive practical knowledge of GMP facility operations, quality requirements, and controlled documentation.
-
Experience overseeing maintenance and calibration programs, using a CMMS, and supporting equipment and facility qualification activities.
-
Direct involvement in regulatory or customer inspections, with the ability to address findings and drive corrective actions.
-
Strong interpersonal judgment, an approachable leadership style, and consistent responsiveness and follow-through.
-
Cold-chain and temperature-controlled manufacturing experience preferred; CFM or PE credentials are a plus.
-
Availability to work onsite in Minnetonka five days per week, with flexibility for occasional travel.
